Canonical Allele Identifier: CA16254067
Gene: SYCP2L HGNC NCBI
COSMIC:
COSN17912674 (not active)
MyVariant.info:
GRCh38 chr6:g.10897255G>A
GRCh37 chr6:g.10897488G>A
gnomAD v2:
6:10897488 G / A
gnomAD v3:
6:10897255 G / A
gnomAD v4:
chr6-10897255-G-A
Joint Max Group AF 0.71506702 (AFR)
Genomes Max Group AF 0.71506702 (AFR)
dbSNP:
2153157
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897255G>A , CM000668.2:g.10897255G>A GRCh38
NC_000006.11:g.10897488G>A , CM000668.1:g.10897488G>A GRCh37
NC_000006.10:g.11005474G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000283141.11:c.337-756G>A MANE Select ENSP00000283141.6:n.337-756G>A
ENST00000283141.10:c.337-756G>A ENSP00000283141.6:n.337-756G>A
ENST00000341041.8:c.337-756G>A ENSP00000340320.4:n.337-756G>A
ENST00000480294.1:c.*299-756G>A ENSP00000417929.1:n.*299-756G>A
ENST00000543878.5:c.334-756G>A ENSP00000440676.2:n.334-756G>A
NM_001040274.2:c.337-756G>A NP_001035364.2:n.337-756G>A
NM_001040274.3:c.337-756G>A MANE Select NP_001035364.2:n.337-756G>A
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